Methanone, (4-chlorophenyl)(5-fluoro-2-hydroxyphenyl)-


Chemical Name: Methanone, (4-chlorophenyl)(5-fluoro-2-hydroxyphenyl)-
CAS Number: 62433-26-5
Product Number: AG00EBA7(AGN-PC-0JLIO6)
Synonyms:
MDL No:
Molecular Formula: C13H8ClFO2
Molecular Weight: 250.6528

Identification/Properties


Properties
MP:
65-69°C(lit.)
BP:
145-152°C at 5 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
250.653g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
250.02g/mol
Monoisotopic Mass:
250.02g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
277
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



$Name$ is a versatile compound frequently utilized in various chemical synthesis processes. This compound, also known as (4-Chlorophenyl)(5-fluoro-2-hydroxyphenyl)methanone, serves as a key building block in the creation of novel pharmaceuticals, agrochemicals, and advanced materials. Its unique structure enables it to participate in a wide range of reactions, leading to the formation of complex organic molecules with enhanced properties.One common application of (4-Chlorophenyl)(5-fluoro-2-hydroxyphenyl)methanone is in the synthesis of bioactive compounds used in drug discovery and development. By incorporating this compound into the molecular structure of pharmaceutical candidates, researchers can modulate their biological activity, improve their pharmacokinetic profile, and enhance their overall efficacy. This compound's presence can also impart specific functional groups or structural motifs necessary for targeting specific biological pathways or interacting with biological macromolecules.Furthermore, (4-Chlorophenyl)(5-fluoro-2-hydroxyphenyl)methanone plays a crucial role in the preparation of intermediate compounds for agrochemicals, enabling the production of crop protection agents with increased selectivity, potency, and environmental compatibility. Its versatility in chemical transformations allows for the synthesis of tailored molecules with desired biological activities and physicochemical properties, contributing to the continuous advancement of the agricultural industry.In the realm of materials science, (4-Chlorophenyl)(5-fluoro-2-hydroxyphenyl)methanone serves as a valuable precursor for the fabrication of functional materials such as polymers, coatings, and catalysts. By incorporating this compound into polymer chains or surface coatings, researchers can impart specific functionalities or enhance material performance, leading to applications in areas such as adhesives, electronics, and catalysis. Its ability to undergo diverse chemical reactions makes it a versatile building block for designing materials with tailored properties for various industrial applications.Overall, the application of (4-Chlorophenyl)(5-fluoro-2-hydroxyphenyl)methanone in chemical synthesis underscores its significance as a pivotal component in the creation of innovative compounds with potential pharmaceutical, agrochemical, and materials applications. Its versatility and reactivity make it a valuable tool for researchers and chemists seeking to develop new molecules with targeted properties and functionalities.